The following data is part of a premarket notification filed by Voss Medical Products with the FDA for Voss Vein Clamp.
| Device ID | K885161 |
| 510k Number | K885161 |
| Device Name: | VOSS VEIN CLAMP |
| Classification | Clamp, Vascular |
| Applicant | VOSS MEDICAL PRODUCTS 7614 LOUIS PASTEUR DRIVE, SUITE 200 San Antonio, TX 78229 |
| Contact | Ron A Voss |
| Correspondent | Ron A Voss VOSS MEDICAL PRODUCTS 7614 LOUIS PASTEUR DRIVE, SUITE 200 San Antonio, TX 78229 |
| Product Code | DXC |
| CFR Regulation Number | 870.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-12-13 |
| Decision Date | 1989-12-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00811304020089 | K885161 | 000 |
| 00811304020058 | K885161 | 000 |